Found: 12
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Protein and functional isoform levels and genetic variants of the BAFF and APRIL pathway components in systemic lupus erythematosus.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15549-0
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- Article
Expression of CD81, SR-BI and LDLR in lymphocytes and monocytes from patients with classic and occult hepatitis C virus infection.
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- Journal of Medical Virology, 2012, v. 84, n. 11, p. 1727, doi. 10.1002/jmv.23345
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- Article
Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases.
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- Human Genetics, 2010, v. 128, n. 2, p. 221, doi. 10.1007/s00439-010-0844-1
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- Article
Association of Functional Polymorphisms of KIR3DL1/DS1 With Behçet's Disease.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02755
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- Article
The complex HLA-E-nonapeptide in Behçet disease.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1080047
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- Article
Monitoring of kinetics and exhaustion markers of circulating CAR-T cells as early predictive factors in patients with B-cell malignancies.
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- Frontiers in Immunology, 2023, p. 01, doi. 10.3389/fimmu.2023.1152498
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- Article
Association of the AIRE gene with susceptibility to rheumatoid arthritis in a European population: a case control study.
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- Arthritis Research & Therapy, 2013, v. 15, n. 1, p. 1, doi. 10.1186/ar4141
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- Article
Mitochondrial DNA A4336G Mutation in Alzheimer’s and Parkinson’s Diseases.
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- European Neurology, 2002, v. 48, n. 1, p. 34, doi. 10.1159/000064955
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- Article
Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci.
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- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0161305
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- Article
Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39113-5
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- Article
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b gene.
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- Human Mutation, 1999, v. 14, n. 6, p. 545, doi. 10.1002/(SICI)1098-1004(199912)14:6<545::AID-HUMU18>3.0.CO;2-J
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- Article
A novel missense mutation 14259 G>A in the mitochondrial NADH dehydrogenase 6 gene (MTND6).
- Published in:
- Human Mutation, 1999, v. 13, n. 3, p. 259, doi. 10.1002/(SICI)1098-1004(1999)13:3<259::AID-HUMU21>3.0.CO;2-F
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- Article